Method and apparatus for analyzing fluid inclusions

ABSTRACT

Method and apparatus for analyzing fluid inclusions. A sectioned mineral sample is mounted on a glass slide and placed in a vacuum chamber. An optical microscope is used to examine the sample through a window in the vacuum chamber to identify a single fluid inclusion. A linear rotary feedthrough includes a diamond stylus on the end thereof that is received in the vacuum chamber. The feedthrough is manipulated by the operator to urge the diamond stylus against the identified fluid inclusion thereby rupturing the same. The gases, including evaporated volatile liquids, released from the inclusion are analyzed by a mass spectrometer.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The instant invention relates to methods and apparatus for analyzingfluid inclusions and more particularly to such methods and apparatus inwhich a fluid inclusion formed in a material such as mineral, glass,semiconducting material and the like is ruptured and the gases releasedtherefrom are analyzed.

2. Setting of the Invention

When natural minerals are formed, fluid present in the vicinity of thecrystal may be trapped in microscopic defects known as fluid inclusions.These fluid inclusions may be ruptured to release the paleofluidscontained therein in order to analyze the same. Such analysis can beused to determine information relating to the nature of the fluidspresent when the mineral was formed.

Analysis of fluid inclusions formed in sedimentary environments canyield information which is useful in the exploration for and productionof oil and gas. For example, such studies can produce informationrelating to timing of hydrocarbon migration relative to rock formation,pathways of hydrocarbon migration, and the influence of hydrocarbons onrock formation.

Fluid inclusions in minerals may be formed at the time of mineral growthor they may form later when cracks in the mineral heal. Fluid inclusionsformed at the time of initial mineral growth are referred to as primaryinclusions and those formed during healing of cracks in thealready-formed mineral are known as secondary inclusions. Cracks whichhave formed and healed at different times in the mineral's past producedifferent generations of secondary inclusions which trap environmentalfluids present at the time of healing of the crack.

Sometimes a mineral overgrowth which acts as a cement may form betweenand around previously-formed mineral growth. Environmental fluids mayalso be trapped in fluid inclusions formed in the cement.

In the past, a number of different techniques have been utilized torelease fluids from the inclusions in minerals and in other substances,such as glass. Such techniques include crushing and drilling. In anothertechnique, the material, for example, a naturally-occurring mineral, isheated thereby increasing the fluid pressure in the fluid inclusionsuntil the same rupture thereby releasing the fluids. This technique isknown in the art as thermal decrepitation. A related technique involvesuse of a laser beam. When the laser beam is directed toward an area ofinterest in the mineral, the fluids in the inclusions are heated therebyrupturing the inclusions and releasing the fluids.

In the past, mass spectrometers have been used to analyze gases releasedfrom fluid inclusions using one of the above-described prior arttechniques. Typically the gases are released by cutting or crushing themineral or by thermal decrepitation. Whatever the technique forreleasing the gas, the gases are released into a vacuum which is incommunication with the mass spectrometer. When the fluids are releasedfrom the inclusions into the vacuum, the volatile liquids in theinclusions evaporate. The gases are provided directly to the massspectrometer where they are ionized and thereafter qualitatively and/orquantitatively analyzed in the usual manner. The mass spectrometer maybe used to to analyze the chemistry of the gases and evaporated volatileliquids and/or to analyze the isotopic ratios of elements containedtherein.

A problem exists with the various prior art methods for releasing fluidsfrom inclusions in naturally-occurring minerals and the like. Whenutilizing techniques such as crushing, slicing and drilling, invariablyfluids from more than one inclusion are released substantiallysimultaneously. This is especially true when dealing with smallinclusions. For example, fluid inclusions of interest in sedimentaryminerals are typically less than 10 microns in diameter. Thus, theanalysis undertaken, whether by mass spectrosocopy or by other means,may be of a plurality of fluid inclusions. Moreover, the analyzed fluidsmay be from inclusions formed at vastly differing times, such as amixture of primary and secondary inclusions or a mixture of differentgenerations of secondary inclusions.

Also, the mineral sample to be analyzed may include a plurality ofdifferent minerals closely adjacent one another as well as mineralgrowth formed between and on the various minerals, all of which includefluid inclusions. When such a sample is crushed, sliced or drilled,fluids from inclusions in different minerals or from one or more cementsmay be simultaneously released. Such techniques prevent accurateanalysis of selected types of inclusions such as inclusions from aparticular mineral or cement or such as only primary inclusions, onlysecondary inclusions, or only a selected generation of secondaryinclusions.

Some theorize that when fluids are released from inclusions innaturally-occurring minerals by thermal decrepitation, single inclusionssequentially burst in response to increasing temperature. However, thereis no known way to verify this. Data generated by mass spectrosocopyanalysis of gases, including evaporated liquids, released from fluidinclusions may be interpreted to mean that (a) only a single inclusionruptured at a specified temperature or (b) groups of inclusions rupturedat a specified temperature.

Even if it could be verified that only a single inclusion at a timeburst as temperature is increased, this technique does not permitselection of a single identified inclusion nor does it permit selectionof one inclusion from among a class of characterized inclusions, such asprimary inclusions, secondary inclusions, a selected generation ofsecondary inclusions, inclusions from a selected cement, etc. In otherwords, as the temperature increases, any of the inclusions in the samplebeing tested may rupture and there exists no control over selection of aparticular fluid inclusion or a fluid inclusion from among a particularclass of inclusions to be ruptured.

The laser technique suffers from similar drawbacks. Typically a selectedarea in a mineral sample is located using a microscope. Thereafter, alaser beam is shined through the microscope onto the sample and the heatgenerated thereby ruptures inclusions in the general area. Although thelaser technique allows exercise of greater control over which inclusionsare to be ruptured than thermal decrepitation of the entire sample, theheat produced by the laser beam is applied to a general area of thesample and it is not possible to limit the technique to rupture only asingle selected inclusion. Thus, the above-described drawbacks of thethermal decrepitation technique are also present when a laser is used torelease gases, including evaporated volatile liquids, from fluidinclusions. In addition, the laser heat can also release gases fromvolatile matter received in cracks in the sample or from adsorbed fluidin the sample. Therefore at least some of the analyzed gas may be fromsources other than fluid inclusions.

There exists a need for a method and apparatus for analyzing fluidinclusions in which a single identified fluid inclusion may be ruptured.

There exists a need for such a method and apparatus in which selectedfluid inclusions from an identified class of inclusions may beselectively ruptured.

There exists a further need for such a method and apparatus in which aplurality of identified fluid inclusions may be individually andsequentially mechanically ruptured.

SUMMARY OF THE INVENTION

The method of the invention comprises the steps of characterizing aclass of fluid inclusions less than 50 microns in diameter formed in anaturally-occurring mineral or the like; identifying a single fluidinclusion within the characterized class; mechanically rupturing theidentified fluid inclusion; and analyzing the gases released from thefluid inclusion.

In another aspect of the invention, a second fluid inclusion within thecharacterized class is identified, mechanically ruptured and theresulting released gases analyzed.

In still another aspect of the method, a fluid inclusion in a samplecontaining a plurality of minerals is identified and mechanicallyruptured and the resulting gases analyzed. Thereafter, a second fluidinclusion formed in a second mineral in the sample is mechanicallyruptured and the gases released therefrom analyzed.

In yet another aspect of the invention, apparatus is provided forperforming the steps of the method.

Additional advantages associated with the instant invention will becomemore fully apparent when the following detailed description is read inview of the accompanying drawings, wherein:

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an enlarged view of a portion of a sectioned mineral samplecontaining a plurality of mineral growths as viewed through amicroscope.

FIG. 2 is a top plan view of apparatus constructed in accordance withthe instant invention.

FIG. 3 is a front view of the apparatus shown in FIG. 2.

FIG. 4 is an enlarged somewhat schematic view, shown partly incross-section, of a portion of the apparatus shown in FIGS. 2 and 3.

FIG. 5 is a schematic view similar to FIG. 4 of an alternativeembodiment of the apparatus of the instant invention.

FIG. 6 is a schematic diagram of a portion of the apparatus of FIGS. 2and 3.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS OF THE INVENTION

Turning now to the drawings and particularly to FIG. 1, considerationwill now be given to an example of a mineral sample containing aplurality of mineral growths. Indicated generally at 10 is a portion ofa sample extracted from naturally-occurring mineral growth. Sample 10consists of a cut section having a thickness of approximately 0.03-1.0millimeter which is polished on both sides and which is mounted on aglass slide (not visible in FIG. 1). The view of FIG. 1 is a view of thepolished section as seen through a microscope and is thus greatlyenlarged. The approximate scale can be indicated in that substantiallyall of the fluid inclusions, like inclusion 12, formed in the variousmineral growths in sample 10 are under 10 microns in diameter. Sample 10includes a plurality of mineral growths, like minerals 14, 16, 18, 10,22, 24. Minerals 16, 18 each include a mineral overgrowth 26, 28 whichacts as and is referred to herein as a cement.

Mineral 24 includes therein a plurality of primary inclusions, likeinclusions 30, 32. These inclusions were formed during the initialgrowth of mineral 24. A healed crack 34 is formed in mineral 24 and ahealed crack 36 is formed in mineral 22 and in mineral 24. Crack 34 wasformed in mineral 24 after the original growth of mineral 24, and thusafter the primary inclusions, like inclusions 30, 32, were formed. Crack36 was also formed in minerals 22, 24 after the formation of the primaryinclusions in both minerals 22, 24. Each of cracks 34, 36 have aplurality of secondary inclusions, as shown, formed therealong. Thesesecondary inclusions were formed during healing of cracks 34, 36 whenmineral growth developed in the cracks. It is to be appreciated that thesecondary inclusions in crack 34 trap environmental fluids at a latertime than the primary inclusions in mineral 24 and the secondaryinclusions along crack 36 trap such fluids at a later time than when theenvironmental fluids were trapped in the primary inclusions in bothminerals 22, 24. Moreover, the secondary inclusions in crack 34 may wellbe formed at a time far removed from those formed in crack 36 and thusthe secondary inclusions in crack 34 may be of a different generationthan those along crack 36. Likewise, the primary inclusions formed inthe various minerals and cements in sample 10 may be formed at vastlydifferent times from one another thus trapping the environmental fluidspresent at the time of formation.

It should be noted that sample 10 may be taken from a portion ofnaturally-occurring mineral growth using the usual sawing and polishingtechniques. After the sample is cut, polished and mounted on a slide,the same may be observed through a microscope to obtain the view ofFIG. 1. Geologists are able to identify, by observation through themicroscope, various types of minerals. Such identification is based onwell know criteria of shape of mineral growth and various opticalproperties. In addition, the fluid inclusions themselves can beclassified in different ways such as the above-described primary andsecondary fluid inclusions. Other categories of inclusionclassifications may be utilized; however, most common is classifying byorigin, namely primary and secondary inclusions. Such inclusions may becharacterized by observation of the sample through the microscope.

Turning now to FIGS. 2 and 3, indicated generally at 38 is apparatusconstructed in accordance with the instant invention. Included thereinis a tube 40 having an ionization chamber 42 mounted on one end thereof,and an ion detector 44 mounted on the other end thereof. A magnet 46 isshown in a solid-line position in FIG. 2 removed to the rear of tube 40and in a dashed-line position about tube 40. A tube 48 is incommunication with ionization chamber 42 and provides a gas sample tothe ionization chamber for analysis. In operative condition a vacuumpump (not shown) maintains a substantial vacuum in tube 40.

That portion of the apparatus shown in FIGS. 2 and 3 which has beendescribed above comprises a commercially available gas spectrometer,such being also referred to herein as means for analyzing gases.Generally speaking, the gas spectrometer operates as follows:

A gas sample to be analyzed is provided to ionization chamber 42 viatube 48. In the ionization chamber an electron beam ionizes the gaseswhich are then accelerated by an electric field along tube 40 towardmagnet 46. The magnetic field alters the direction of travel of the ionsin tube 40 depending upon the electrical charge and mass of each ion andupon the strength of the magnetic field. Ions of a certainmass-to-charge ratio travel around the bend in tube 40 toward detector44. Other ions strike the walls of tube 40 and are not ultimatelydetected. The foregoing description of the operation of the massspectrometer describes in general the operation of commerciallyavailable mass spectrometers. Such mass spectrometers may be used toanalyze gases present and to analyze isotope ratios of elements in thegases.

A vacuum chamber 50 is in fluid communication with ionization chamber 42via tube 48. A commercially available microscope 52 is positioned overvacuum chamber 50. For a more detailed view of vacuum chamber 50,attention is directed to FIG. 4.

Chamber 50 is in fluid communication with ionization chamber 42 via tube48. As mentioned, tube 40 of the mass spectrometer is maintained in asubstantial vacuum by a pump (not shown) and thus tube 48 and chamber 50are also maintained in a vacuum.

Sample 10, as will be recalled, is mounted on a glass slide 54 which isviewable in FIG. 4. Slide 54, in the view of FIG. 4 is tilted forward toshow sample 10. In operative condition, the slide is substantiallyparallel to the upper and lower walls of chamber 50. Slide 54 isremoveably mounted on a commercially available manipulator 56 whichenables the slide to be moved laterally and vertically responsive to acommercially available operator control (not shown) for the manipulator.Chamber 50 includes a glass window 58 formed in an upper wall thereofover which is positioned a lower housing 60 of microscope 52. A lowerwindow 62 is formed in a lower wall of vacuum chamber 50 beneath window58. A light 64 is positioned beneath window 62.

Indicated generally at 66 is a rotary linear feedthrough. Feedthrough 66includes a shaft 68 which extends through a seal 70. The lower end ofthe shaft is connected to an arm 72. A diamond stylus 74 is mounted onthe end of arm 72 and is positioned so that a point formed thereon isdirected downwardly.

Shaft 68, when rotated under operator control, imparts rotary motion toarm 72 about the axis of shaft 68. Also, the operator may raise andlower shaft 68 to effect raising and lowering of arm 72.

Attention is next directed to FIG. 5 wherein the structure previouslyidentified with a numeral herein retains the same number in FIG. 5. Inthe embodiment of FIG. 5, a diamond stylus 76 is mounted directly on theunderside of window 58 above sample 10 with a point formed on the stylusbeing directed downwardly.

Turning now to FIG. 6, ion detector 44 includes therein a pair ofcommercially available Gallileo-type electron multipliers 78, 80. Eachof the electron multipliers is connected to an associated ion counter82, 84 which in turn are connected to a commercially available computer86. The end of tube 40 which is directed toward ion detector 44 includesan end plate 87 having slits, such as slits 88, 90 formed therein. Endplate 87 may be fixed in selected positions relative to tube 40 therebyvaring the radial position of the slits relative to the longitudinalaxis of tube 40.

Consideration will now be given to the operation of the instantembodiments of the invention. When a mineral growth of interest islocated, sample 10 is prepared in the usual fashion. A slice is takenfrom the mineral growth and is thereafter polished and mounted on glassslide 54, as shown in FIG. 4 and 5. Thereafter, slide 54 is mounted onmanipulator 56 and light 64 is turned on. An operator examines sample 10through microscope 52 and positions the same beneath the microscope lensusing the controls (not shown) for manipulator 56. The operator searchesfor a class of fluid inclusions of interest, for example, the secondaryinclusions along healed crack 36 in FIG. 1. Next a single fluidinclusion of interest is identified. Feedthrough 66 is manipulated byrotation of shaft 68 until stylus 74 is above the identified fluidinclusion. Manipulator 56 may also be moved in order to position theslide relative to stylus 74.

When the feedthrough and slide are positioned as described above, shaft68 is urged downwardly until diamond stylus 74 punctures the identifiedfluid inclusion thereby releasing gases and evaporated volatile liquidsfrom the inclusion. It is to be appreciated that fluid inclusions mayinclude mixtures of gases and liquids, and in some cases solids.Volatile liquids are those which evaporate when exposed to the vacuumwithin chamber 50.

When the inclusion is so ruptured, the gases released from theinclusion, including the evaporated volatile liquids, pass through tube48 to ionization chamber 42 where the same are ionized. The ionizedgases are accelerated in tube 40 toward magnet 46 which changes thedirection of travel of the ionized gases.

Most fluid inclusions of interest in connection with exploration andproduction of oil and gas are water dominated. In water, the isotoperatios of most interest, and those which have the best chance of beinganalyzed, are ¹⁶ O/¹⁸ O ¹ H/² H. These ratios can be determined bydetecting the following ionic species: H₂ ¹⁶ O⁺, HD¹⁶ O+, and H₂ ¹⁸ O⁺.

The mass spectrometer is adjusted, by adjusting the power of magnet 46,so that ionic species having a mass to charge ratio of 18, 19, and 20,namely H₂ ¹⁶ O⁺, HD¹⁶ O⁺, and H₂ ¹⁸ O⁺, strike end plate 87.

In FIG. 6, a first ion stream 92 is made up of H₂ ¹⁶ O⁺ ions; a secondstream 94 is made up of HD¹⁶ O⁺ ions and a third ion stream 96 is madeup H₂ ¹⁸ O⁺ ions Because each ion stream is made up of ions having adifferent mass-to-charge ratio, the effect of magnet 46 on the ions isto separate them into very slightly non-parallel streams of ions, eachof which strikes end plate 87 in a pre-determined location. It can thusbe seen that by selectively positioning end plate 87 and electronmultipliers 78, 80, an ion stream made up of ions having a selectedmass-to-charge ratio may be directed into one of the electronmultipliers while the other ions are absorbed in end plate 87. Each ionin, for example, ion stream 92, which passes through slit 88 and strikeselectron multiplier 78 generates a shower of secondary electrons inmultiplier 78 which is provided to ion counter 82. Each electron showeris counted by counter 82 as a single ionization event which is recordedby computer 86.

Detector 44 is advantageous when dealing with a very small gas sample,such as that which is released from a single fluid inclusion. Sinceelectron multipliers do not necessarily release the same number ofelectrons in response to ions having the same mass-to-charge ratio, useof the ion counters to convert each electron shower into a singleionization event increases the accuracy of the collected data. It can beseen that by shifting end plate 87 and electron multipliers 78, 80,different selected ion streams may be detected. Furthermore, by changingthe strength of the magnetic field generated by magnet 46, streams ofions having different mass-to-charge ratios than those shown in theexample may be made to strike end plate 87 and/or pass through the slitstherein.

Referring now to FIG. 5, in the operation of the embodiment showntherein, slide manipulator 56 is positioned until the fluid inclusion ofinterest is directly beneath diamond stylus 76. Thereafter, the controls(not shown) for manipulator 56 are operated to drive manipulator 56, andthus sample 10, directly upwardly into diamond stylus 76. Such rupturesthe fluid inclusion positioned beneath the diamond stylus and permitsthe gases released therefrom to be analyzed as described above. Inoperation of the embodiment of FIG. 5, an operator uses microscope 52 inthe same manner as the embodiment of FIG. 4 to characterize a class ofinclusions and to thereafter identify a particular inclusion for rupturein order to analyze the gases released therefrom.

Each diamond stylus 74, 76 includes a point sufficient to puncture fluidinclusions less than 10 microns in diameter.

It can thus be seen that the instant invention permits characterizing aclass of fluid inclusions such as primary or secondary inclusions, forexample, by observation (in the instant embodiment of the invention withan optical microscope) and thereafter identifying a single inclusionwithin the characterized class. The identified inclusion may then beruptured and the gases released therefrom analyzed to derive informationrelating to the geologic process which formed the mineral containing thefluid inclusion.

The instant invention may therefore be used to verify whether or notprior art techniques for analyzing gases released from fluid inclusions,such as thermal decrepitation, are in fact sequentially and individuallyreleasing gases from fluid inclusions as is theorized by some. Moreover,the instant invention permits selecting a single particular identifiedfluid inclusion for rupturing in order to analyze gases releasedtherefrom so that data from a particular characterized class ofinclusions may be generated. Generating such data was not possible withthe prior art techniques for releasing gases from fluid inclusions.

It is to be appreciated that additions and modifications may be made tothe embodiments of the invention disclosed herein without departing fromthe spirit of the same which is defined in the following claims.

What is claimed is:
 1. A method for deriving information relating togeologic processes which form naturally-occurring mineral useful in theexploration of oil and gas, said method comprising the stepsof:providing a sample comprising a cut polished section of sedimentaryrock containing a plurality of microscopic fluid inclusions of less than50 microns in diameter, the fluid inclusions being of interest in theexploration for oil and gas; characterizing a class of said microscopicfluid inclusions of less than 50 microns in diameter which are formed insuch sample; identifying and selecting in the sample a singlemicroscopic fluid inclusion within said characterized class;mechanically rupturing in the sample essentially only the identified andselected microscopic fluid inclusion; and analyzing gases released fromsaid fluid inclusion.
 2. The method of claim 1, wherein said methodfurther includes the steps of:identifying and selecting a secondmicroscopic fluid inclusion in the sample within said characterizedclass; mechanically rupturing in the sample essentially only theidentified and selected second microscopic fluid inclusion; andanalyzing gases released from the second fluid inclusion.
 3. The methodof claim 2, wherein the sample includes a cement overgrowth formed onsaid mineral and wherein said method further comprises the stepsof:identifying and selecting a single microscopic fluid inclusion ofless than 50 microns in diameter formed in said cement overgrowth;mechanically rupturing essentially only the identified and selectedcement fluid inclusion; and analyzing gases released from the cementfluid inclusion.
 4. The method of claim 3 wherein the sample includes asecond cement overgrowth formed on said mineral and wherein said methodfurther comprises the steps of:identifying and selecting a singlemicroscopic fluid inclusion of less than 50 microns in diameter formedin said second cement overgrowth; mechanically rupturing essentiallyonly the identified and selected second cement fluid inclusion; andanalyzing gases released from the second cement fluid inclusion.
 5. Themethod of claim 2 wherein said class of fluid inclusions comprises onlyprimary fluid inclusions.
 6. The method of claim 5 wherein said class offluid inclusions comprises only a user-selected generation of primaryfluid inclusions.
 7. The method of claim 2 wherein said class of fluidinclusions comprises only secondary fluid inclusions.
 8. The method ofclaim 7 wherein said class of fluid inclusions comprises only auser-selected generation of secondary fluid inclusions.
 9. The method ofclaim 1 wherein said method further comprises the stepsof:characterizing a second class, different from the first class, ofmicroscopic fluid inclusions which are formed in the mineral in a samplecomprising the mineral; identifying and selecting in the sample a singlemicroscopic fluid inclusion within said second characterized class;mechanically rupturing in the sample essentially only the identified andselected microscopic fluid inclusion within said second characterizedclass; and analyzing gases released from said second class fluidinclusion.
 10. The method of claim 9 wherein said method furthercomprises the steps of:identifying and selecting a plurality ofmicroscopic fluid inclusions of less than 50 microns in diameter withineach of said characterized classes; individually and sequentiallymechanically rupturing each of such identified and selected fluidinclusions; and analyzing gases released from each of such rupturedfluid inclusions.
 11. The method of claim 10 wherein the step ofindividually and sequentially mechanically rupturing each of suchidentified fluid inclusions comprises the steps of:individually andsequentially mechanically rupturing each of such identified fluidinclusions in said first characterized class; and thereafter,individually and sequentially rupturing each of such identified fluidinclusions in said second characterized class.
 12. The method of claim 9further comprising:determining from resulting data at least one selectedfrom the group consisting of of timing of hydrocarbon migration relativeto rock formation, pathways of hydrocarbon migration, and influence ofhydrocarbons on rock formation.
 13. The method of claim 1, wherein thestep of selecting a single inclusion comprises the steps of:examiningthe sample with a microscope; and locating the selected inclusion withthe microscope.
 14. The method of claim 1 wherein the step of analyzingthe gases released from the inclusion comprises the step of subjectingthe gases to mass spectrometric analysis.
 15. The method of claim 14wherein the step of subjecting the gases to mass spectrometric analysisincludes the step of evaporating all volatile liquids released from theinclusion.
 16. The method of claim 15 wherein the step of evaporatingall volatile liquids in the inclusion comprise the step of evaporatingwater in the inclusion.
 17. The method of claim 16 wherein the step ofsubjecting such evaporated liquids and all gases released from theinclusion to mass spectrometric analysis comprises the step of determingthe isotopic ratios of selected elements in such evaporated liquids andgases.
 18. The method of claim 17 wherein the step of determining theisotopic ratios of selected elements in such evaporated liquids andgases comprises the step of determining the ¹⁶ O/¹⁸ O ratio or the ¹ H/²H.
 19. The method of claim 14 wherein the step of subjecting the gasesto mass spectrometric analysis comprises the step of determining theisotopic ratios of selected elements in the gases.
 20. The method ofclaim 14 wherein the identified and selected fluid inclusion is lessthan 10 microns in diameter.
 21. The method of claim 1 wherein the stepof analyzing gases includes the step of evaporating volatile liquidsfrom the fluid inclusion.
 22. The method of claim 1 wherein theidentified and selected fluid inclusion is less than 10 microns indiameter.
 23. The method of claim 1 wherein the cut polished section hasa thickness of about 0.3 to about 1.0 millimeters.